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(+)-MENTHOL

  • CAS No.: 15356-60-2
  • Purity: 99%
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Manufacturer supply top purity (+)-MENTHOL 15356-60-2 with ISO standards

  • Molecular Formula: C10H20O
  • Molecular Weight: 156.268
  • Vapor Pressure: 0.8 mm Hg ( 20 °C) 
  • Melting Point: 43-44 °C(lit.) 
  • Refractive Index: 50 ° (C=10, EtOH) 
  • Boiling Point: 215.383 °C at 760 mmHg 
  • PKA: 15.30±0.60(Predicted) 
  • Flash Point: 93.333 °C 
  • PSA: 20.23000 
  • Density: 0.89 g/cm3 
  • LogP: 2.43950 

(+)-MENTHOL(Cas 15356-60-2) Usage

General Description

(1S,2R,5S)-(+)-menthol is a chiral secondary alcohol. Its alcohol group can be protected as 2-tetrahydrofuranyl ether by reacting with bromotrichloromethane and tetrahydrofuran.

InChI:InChI=1/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10+/m1/s1

15356-60-2 Relevant articles

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Read,Grubb

, p. 188,193 (1931)

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Enantioselective Hydrolysis of D,L-Menthyl Benzoate to L-(-)-Menthol by Recombinant Candida rugosa Lipase LIP1

Vorlova, Sandra,Bornscheuer, Uwe T.,Gatfield, Ian,Hilmer, Jens-Michael,Bertram, Heinz-Juergen,Schmid, Rolf D.

, p. 1152 - 1155 (2002)

The stereoselective synthesis of L-menth...

Stereoselective reduction of menthone by molecularly imprinted polymers

Hedin-Dahlstroem, Jimmy,Shoravi, Siamak,Wikman, Susanne,Nicholls, Ian A.

, p. 2431 - 2436 (2004)

Polymeric chiral reductants selective fo...

Enantioselective enzymatic resolution of racemic alcohols by lipases in green organic solvents

Belafriekh, Abderahmane,Secundo, Francesco,Serra, Stefano,Djeghaba, Zeineddine

, p. 473 - 478 (2017)

The effects of two eco-friendly solvents...

Apple-tree shoots and transformed carrot and apple roots used as biocatalysts in enantioselective acetate hydrolysis, alcohol oxidation and ketone reduction

Mironowicz, Agnieszka,Kromer, Krystyna

, p. 1655 - 1662 (1998)

(±)-1-Phenylethyl (1), (±)-1-(1-naphthyl...

Novel highly efficient absolute optical resolution method by serial combination of two asymmetric reactions from acetylene monomers having racemic substituents

Aoki, Toshiki,Kaneko, Takashi,Liu, Lijia,Suzuki, Junpei,Tang, Yanan,Teraguchi, Masahiro

supporting information, p. 450 - 461 (2022/01/15)

For general optical resolution, an optic...

Continuous synthesis of menthol from citronellal and citral over Ni-beta-zeolite-sepiolite composite catalyst

Er?nen, Kari,M?ki-Arvela, P?ivi,Martinez-Klimov, Mark,Muller, Joseph,Murzin, Dmitry Yu.,Peurla, Markus,Simakova, Irina,Vajglova, Zuzana

, (2022/04/03)

One-pot continuous synthesis of menthols...

Light-Induced Formation/Scission of C-N, C-O, and C-S Bonds Enables Switchable Stability/Degradability in Covalent Systems

Hai, Yu,Li, Ziyi,Lu, Hanwei,Ye, Hebo,You, Lei,Zou, Hanxun

supporting information, p. 20368 - 20376 (2021/12/03)

The manipulation of covalent bonds could...

Heterogeneous Hydroxyl-Directed Hydrogenation: Control of Diastereoselectivity through Bimetallic Surface Composition

Shumski, Alexander J.,Swann, William A.,Escorcia, Nicole J.,Li, Christina W.

, p. 6128 - 6134 (2021/05/29)

Directed hydrogenation, in which product...

15356-60-2 Process route

(+/-)-menthone
491-07-6,1074-95-9,1196-31-2,3391-87-5,10458-14-7,14073-97-3,18309-28-9,36977-92-1,117773-78-1,89-80-5,17627-49-5,7786-64-3

(+/-)-menthone

phenyl isopropyl ketone
611-70-1

phenyl isopropyl ketone

rac-2-methyl-1-phenylpropan-1-ol
611-69-8

rac-2-methyl-1-phenylpropan-1-ol

2-isopropyl-5-methylcyclohexan-1-ol
89-78-1,490-99-3,491-01-0,491-02-1,1490-04-6,2216-51-5,2216-52-6,3623-51-6,3623-52-7,3623-53-8,15356-60-2,15356-70-4,20747-49-3,20752-33-4,20752-34-5,23283-97-8,64282-88-8

2-isopropyl-5-methylcyclohexan-1-ol

Conditions
Conditions Yield
With bis(2,6-di-tert-butyl-4-methylphenoxide)methylaluminum; diisobutylaluminium hydride; at -78 ℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
succinic acid anhydride
108-30-5

succinic acid anhydride

menthol
15356-70-4

menthol

(1S,2R,5S)-(+)-menthol
15356-60-2

(1S,2R,5S)-(+)-menthol

(-)-menthol
2216-51-5

(-)-menthol

L-menthylsuccinic acid
77341-67-4

L-menthylsuccinic acid

4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid
204326-53-4

4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

Conditions
Conditions Yield
With Candida cylindracea lipase; In diethyl ether; at 20 ℃; for 24h; Schlenk technique; Resolution of racemate; Enzymatic reaction;
53 % ee
25 % ee

15356-60-2 Upstream products

  • 10458-14-7
    10458-14-7

    (2R,5S)-menthone

  • 1196-31-2
    1196-31-2

    (1R,4R)-(+)-isomenthone

  • 15356-70-4
    15356-70-4

    menthol

  • 10458-14-7
    10458-14-7

    Menthone

15356-60-2 Downstream products

  • 2085-26-9
    2085-26-9

    di-((1S )-menthyl)-oxalate

  • 2085-26-9
    2085-26-9

    ((1R )-menthyl)-((1S )-menthyl)-oxalate

  • 149126-05-6
    149126-05-6

    phenylcarbamic acid-((1S )-menthyl ester)

  • 91796-57-5
    91796-57-5

    4-Methyl-benzenesulfinic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester

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